Replication Medical, Inc.
Country not established
- Devices
- 1
What Replication Medical, Inc. makes
Replication Medical, Inc. manufactures the Vessel Guard, a device designed to protect blood vessels during surgical procedures, reducing the risk of complications such as perforation or occlusion.
The Vessel Guard is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Replication Medical Vessel Guard Ref K082782
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Replication Medical, Inc. have in the registry?
The registry currently lists 1 device for Replication Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Replication Medical, Inc.'s devices?
Among its 1 most recently registered device, Replication Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Replication Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Replication Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Replication Medical, Inc. in the registry?
The most recently registered devices listed for Replication Medical, Inc. include REPLICATION MEDICAL VESSEL GUARD.